Interrogating ligand-receptor interactions using highly sensitive cellular biosensors

Interactions of membrane-resident proteins are important targets for therapeutic interventions but most methods to study them are either costly, laborious or fail to reflect the physiologic interaction of membrane resident proteins in trans. Here we describe highly sensitive cellular biosensors as a...

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Veröffentlicht in:Nature communications 2023-11, Vol.14 (1), p.7804-7804, Article 7804
Hauptverfasser: Funk, Maximilian A., Leitner, Judith, Gerner, Marlene C., Hammerler, Jasmin M., Salzer, Benjamin, Lehner, Manfred, Battin, Claire, Gumpelmair, Simon, Stiasny, Karin, Grabmeier-Pfistershammer, Katharina, Steinberger, Peter
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Sprache:eng
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Zusammenfassung:Interactions of membrane-resident proteins are important targets for therapeutic interventions but most methods to study them are either costly, laborious or fail to reflect the physiologic interaction of membrane resident proteins in trans. Here we describe highly sensitive cellular biosensors as a tool to study receptor-ligand pairs. They consist of fluorescent reporter cells that express chimeric receptors harboring ectodomains of cell surface molecules and intracellular signaling domains. We show that a broad range of molecules can be integrated into this platform and we demonstrate its applicability to highly relevant research areas, including the characterization of immune checkpoints and the probing of cells for the presence of receptors or ligands. The platform is suitable to evaluate the interactions of viral proteins with host receptors and to test for neutralization capability of drugs or biological samples. Our results indicate that cellular biosensors have broad utility as a tool to study protein-interactions. The interaction of membrane-resident proteins plays an essential role in biological processes. Here the authors describe cellular biosensors based on chimeric receptors, as a tool to study the interaction of receptor-ligand pairs such as immune checkpoint molecules or virus attachment proteins and their receptors.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-43589-1